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Published on: March 10, 2015
Synergistic Inhibition of Colorectal Cancer Cells by Autocrine Motility Factor Peptide and Glycyrrhetinic Acid
Se Gie Kim1, Thanh Van Duong2, Semin Lee3
1Department of Cosmetic Science, Kyungsung University, 48434 Busan, Republic of Korea.
Background:
Anti-cancer peptides are a powerful drug concept that induces cancer cell death through growth inhibition and membrane disruption, providing broad efficacy. The autocrine motility factor (AMF) interacts with the AMF receptor, regulating cancer cell motility, proliferation, metastasis, and angiogenesis through autocrine and paracrine pathways. However, studies verifying the synergistic effect of the combined use of anti-cancer drugs extracted from plants and AMF treatment are insufficient.
Methods:
The effects of AMF-derived peptide sequences were evaluated in HT29 and SW620 colorectal cancer (CRC) cell lines. The study assessed the impact of AMF peptides on cell proliferation, colony formation, the Nicotinamide Adenine Dinucleotide Phosphate/Reduced Nicotinamide Adenine Dinucleotide Phosphate (NADP+/NADPH) ratio, and reactive oxygen species (ROS) generation in these CRC cells. Additionally, the combined effect of AMF peptides and glycyrrhetinic acid (GA), a compound derived from licorice plants, was investigated by analyzing cell proliferation, colony formation, ROS production, and cell cycle progression in CRC cells.
Results:
AMF peptides significantly inhibited CRC cell growth (p < 0.05), decreased colony formation (p < 0.05), and increased the NADP+/NADPH ratio (p < 0.05) and ROS production (p < 0.001). When combined with GA, AMF peptides enhanced GA's effects on CRC cells, further suppressing cell growth (p < 0.05) and colony formation (p < 0.05) while increasing ROS generation (p < 0.05).
Conclusion:
The synergy between AMF peptides and GA, derived from licorice plants, suggests the potential for combined peptide-phytochemical therapy for treating CRC.
Insights
This study shows that autocrine motility factor (AMF) peptides combined with glycyrrhetinic acid (GA) from licorice plants synergistically inhibit colorectal cancer (CRC) cell growth and colony formation by increasing reactive oxygen species (ROS). This suggests a potential new peptide-phytochemical therapy for CRC.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Anti-cancer peptides offer broad efficacy by inducing cancer cell death.
- Autocrine motility factor (AMF) regulates cancer cell processes.
- Synergistic effects of plant-derived anti-cancer compounds and AMF are understudied.
Purpose of the Study:
- To evaluate AMF-derived peptides' effects on colorectal cancer (CRC) cells.
- To investigate the synergistic impact of AMF peptides combined with glycyrrhetinic acid (GA) on CRC.
Main Methods:
- Assessed AMF peptides' effects on CRC cell proliferation, colony formation, NADP+/NADPH ratio, and ROS generation.
- Investigated combined AMF peptides and GA effects on CRC cell proliferation, colony formation, ROS production, and cell cycle progression.
Main Results:
- AMF peptides significantly inhibited CRC cell growth and colony formation (p < 0.05).
- AMF peptides increased the NADP+/NADPH ratio and ROS production (p < 0.05 and p < 0.001, respectively).
- Combined AMF peptides and GA enhanced GA's anti-cancer effects, further suppressing growth and colony formation while increasing ROS (p < 0.05).
Conclusions:
- AMF peptides demonstrate anti-cancer properties against CRC cells.
- Synergy observed between AMF peptides and GA suggests potential for combined peptide-phytochemical therapy in CRC treatment.
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